Bioprospecting and Molecular Pharmacology Laboratory, Rajiv Gandhi Centre for Biotechnology, Thiruvananthapuram, India.
J Ethnopharmacol. 2012 Jan 31;139(2):359-65. doi: 10.1016/j.jep.2011.11.012. Epub 2011 Nov 26.
Glycosmis pentaphylla (Retz.) Correa is used in Indian traditional medicine against jaundice and other liver disorders.
The study aims to determine the in vitro anticancer and apoptosis inducing activity of Glycosmis pentaphylla in hepatocellular carcinoma cell line, Hep3 B.
The cytotoxic and apoptosis inducing activity of the crude extract and active fractions were estimated on Hep3 B and RAW264.7 cell lines by MTT assay, Hoechst staining, DNA fragmentation, morphological studies, reverse transcription polymerase chain reaction and anti-poly-(ADP-ribose)-polymerase assays. The phytochemical profiling of active extract was done by TLC and HPTLC methods.
Ethanol extract of Glycosmis pentaphylla was more effective than other extracts in reducing the proliferation of Hep3 B cells. As revealed by the results from DNA fragmentation, Hoechst staining, morphological studies, RT-PCR, PARP cleavage and gene expression studies, active extract induced apoptosis on Hep3 B cell line in concentration and time dependent manner with increase in the Bax/Bcl2 gene expression ratio. Chemo profiling data revealed the presence of flavonoid in the active fraction.
The study showed that major active component in the ethanol extract of Glycosmis pentaphylla is a flavonoid which induces apoptosis on cancer cell line, Hep3 B, by increasing the expression ratio of Bax/Bcl2 genes in a time and dose dependent manner.
五叶甘橘(Retz.)Correa 被用于印度传统医学中治疗黄疸和其他肝脏疾病。
本研究旨在确定五叶甘橘在肝癌细胞系 Hep3B 中的体外抗癌和诱导细胞凋亡活性。
通过 MTT 测定法、Hoechst 染色、DNA 片段化、形态学研究、逆转录聚合酶链反应和抗聚(ADP-核糖)聚合酶测定法,评估粗提取物和活性馏分对 Hep3B 和 RAW264.7 细胞系的细胞毒性和诱导细胞凋亡活性。用 TLC 和 HPTLC 方法对活性提取物进行植物化学分析。
五叶甘橘的乙醇提取物比其他提取物更有效地抑制 Hep3B 细胞的增殖。DNA 片段化、Hoechst 染色、形态学研究、RT-PCR、PARP 切割和基因表达研究的结果表明,活性提取物以浓度和时间依赖的方式诱导 Hep3B 细胞系发生凋亡,同时 Bax/Bcl2 基因表达比值增加。化学特征数据显示活性部分存在黄酮类化合物。
本研究表明,五叶甘橘乙醇提取物中的主要活性成分是一种黄酮类化合物,它通过增加 Bax/Bcl2 基因的表达比值,以时间和剂量依赖的方式诱导癌细胞系 Hep3B 发生凋亡。